Linked Data
dbSNP Id:
rs1814140770
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.127343304_127343305insC , CM000670.2:g.127343304_127343305insC | GRCh38 |
| NC_000008.10:g.128355550_128355551insC , CM000670.1:g.128355550_128355551insC | GRCh37 |
| NC_000008.9:g.128424732_128424733insC | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000645438.1:c.-560+3869_-560+3870insC (POU5F1B) | ENSP00000495779.1:n.-560+3869_-560+3870insC | |
| NR_117099.1:n.457+3869_457+3870insC (CASC21) | ||
| NR_117100.1:n.1177-53245_1177-53244insG (CASC8) |